Resultats de la cerca - Xuyu Cai

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  1. 1
    Somatic Mutation, Genomic Variation, and Neurological Disease

    Somatic Mutation, Genomic Variation, and Neurological Disease per Annapurna Poduri, Gilad D. Evrony, Xuyu Cai, Christopher A. Walsh

    Publicat 2013
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  2. 2
    A Proximal Centriole-Like Structure Is Present in Drosophila Spermatids and Can Serve as a Model to Study Centriole Duplication

    A Proximal Centriole-Like Structure Is Present in Drosophila Spermatids and Can Serve as a Model to Study Centriole Duplication per Stéphanie Blachon, Xuyu Cai, Kela A Roberts, Kevin Yang, Andrey Polyanovsky, Allen Church, Tomer Avidor‐Reiss

    Publicat 2009
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  3. 3
    Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain

    Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain per Xuyu Cai, Gilad D. Evrony, Hillel S. Lehmann, Princess C. Elhosary, Bhaven K. Mehta, Annapurna Poduri, Christopher A. Walsh

    Publicat 2014
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  4. 4
    Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain

    Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain per Xuyu Cai, Gilad D. Evrony, Hillel S. Lehmann, Princess C. Elhosary, Bhaven K. Mehta, Annapurna Poduri, Christopher A. Walsh

    Publicat 2015
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  5. 5
    Cell Lineage Analysis in Human Brain Using Endogenous Retroelements

    Cell Lineage Analysis in Human Brain Using Endogenous Retroelements per Gilad D. Evrony, Eun‐Jung Lee, Bhaven K. Mehta, Yuval Benjamini, Robert M. Johnson, Xuyu Cai, Lixing Yang, Psalm Haseley, Hillel S. Lehmann, Peter J. Park, Christopher A. Walsh

    Publicat 2015
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  6. 6
    Enrichment of short mutant cell-free DNA fragments enhanced detection of pancreatic cancer

    Enrichment of short mutant cell-free DNA fragments enhanced detection of pancreatic cancer per Xiaoyu Liu, Lingxiao Liu, Yuan Ji, Changyu Li, Tao Wei, Xuerong Yang, Yuefang Zhang, Xuyu Cai, Yangbin Gao, Weihong Xu, Shengxiang Rao, Dayong Jin, Wenhui Lou, Zilong Qiu, Xiaolin Wang

    Publicat 2019
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  7. 7
    Targeted and genome-wide sequencing reveal single nucleotide variations impacting specificity of Cas9 in human stem cells

    Targeted and genome-wide sequencing reveal single nucleotide variations impacting specificity of Cas9 in human stem cells per Luhan Yang, Dennis Grishin, Gang Wang, John Aach, Cheng‐Zhong Zhang, Raj Chari, Jason Homsy, Xuyu Cai, Yue Zhao, Jian‐Bing Fan, Christine E. Seidman, Jonathan G. Seidman, William T. Pu, George M. Church

    Publicat 2014
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  8. 8
    A novel cell‐free DNA methylation‐based model improves the early detection of colorectal cancer

    A novel cell‐free DNA methylation‐based model improves the early detection of colorectal cancer per Xianrui Wu, Yunfeng Zhang, Tuo Hu, Xiaowen He, Yifeng Zou, Qiling Deng, Jia Ke, Lei Lian, Xiaosheng He, Dezhi Zhao, Xuyu Cai, Zhiwei Chen, Xiaojian Wu, Jian‐Bing Fan, Feng Gao, Ping Lan

    Publicat 2021
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  9. 9
    Non-invasive diagnosis of early-stage lung cancer using high-throughput targeted DNA methylation sequencing of circulating tumor DNA (ctDNA)

    Non-invasive diagnosis of early-stage lung cancer using high-throughput targeted DNA methylation sequencing of circulating tumor DNA (ctDNA) per Wenhua Liang, Yue Zhao, Weizhe Huang, Yangbin Gao, Weihong Xu, Jinsheng Tao, Meng Yang, Lequn Li, Ping Wei, Hui Shen, Xiangning Fu, Zhiwei Chen, Peter W. Laird, Xuyu Cai, Jian‐Bing Fan, Jianxing He

    Publicat 2019
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  10. 10
    Somatic mutation in single human neurons tracks developmental and transcriptional history

    Somatic mutation in single human neurons tracks developmental and transcriptional history per Michael A. Lodato, Mollie B. Woodworth, Semin Lee, Gilad D. Evrony, Bhaven K. Mehta, Amir Karger, Soohyun Lee, Thomas W. Chittenden, Alissa M. D’Gama, Xuyu Cai, Lovelace J. Luquette, Eunjung Lee, Peter J. Park, Christopher A. Walsh

    Publicat 2015
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  11. 11
    Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly

    Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly per Fowzan S. Alkuraya, Xuyu Cai, Carina Emery, Ganeshwaran H. Mochida, Mohammed S. Al‐Dosari, Jillian M. Felie, R. Sean Hill, Brenda J. Barry, Jennifer N. Partlow, Generoso G. Gascon, Amal Y. Kentab, Mohammed M. Jan, Ranad Shaheen, Yuanyi Feng, Christopher A. Walsh

    Publicat 2011
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  12. 12
    Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations

    Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations per Annapurna Poduri, Gilad D. Evrony, Xuyu Cai, Princess C. Elhosary, Rameen Beroukhim, Maria K. Lehtinen, L. Benjamin Hills, Erin L. Heinzen, Anthony D. Hill, R. Sean Hill, Brenda J. Barry, Blaise F. D. Bourgeois, James J. Riviello, A. James Barkovich, Peter McL. Black, Keith L. Ligon, Christopher A. Walsh

    Publicat 2012
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  13. 13
    Development and Validation of an Ultradeep Next-Generation Sequencing Assay for Testing of Plasma Cell-Free DNA from Patients with Advanced Cancer

    Development and Validation of an Ultradeep Next-Generation Sequencing Assay for Testing of Plasma Cell-Free DNA from Patients with Advanced Cancer per Filip Janků, Shile Zhang, Jill Waters, Li Liu, Helen J. Huang, Vivek Subbiah, David S. Hong, Daniel D. Karp, Siqing Fu, Xuyu Cai, Nishma M. Ramzanali, Kiran Madwani, Goran Cabrilo, Debra L. Andrews, Yue Zhao, Milind Javle, Scott Kopetz, Rajyalakshmi Luthra, Hyunsung J. Kim, Sante Gnerre, Ravi Vijaya Satya, Han-Yu Chuang, Kristina M. Kruglyak, Jonathan Toung, Chen Zhao, Richard Shen, John V. Heymach, Funda Meric‐Bernstam, Gordon B. Mills, Jian-Bing Fan, Neeraj Salathia

    Publicat 2017
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